雌性根田鼠断奶后对亲本尿气味的记忆

为研究亲子分开后雌性根田鼠对亲本气味的记忆持续时间，分别在未分开（20日龄）、分开10 d（30日龄）、20 d（40日龄）、30 d（50日龄）、40 d（60日龄）时，以新鲜尿作气味源，在行为观察箱中记录雌性根田鼠对不同气味源的行为响应模式，结果表明：(1) 未分开时，雌鼠遭遇父本气味时自我修饰的频次极显著高于陌生雄鼠气味，在分开10 d时，雌鼠接近父本气味的频次显著多于接近陌生雄鼠气味的频次，其对前者反标记显著少于后者；(2)分开20 d后，雌鼠对父本和陌生雄鼠气味的行为响应无明显差异；(3) 未分窝时，雌性根田鼠幼仔对母本和陌生雌鼠气味的行为响应无差异；（4）分开10—40 d时，雌性根田鼠对母本和陌生雌鼠气味表现出不同的行为响应模式。以上结果表明，在亲子分开10 d时，雌鼠仍能识别父本和陌生雄鼠的气味；分开20 d后，雌鼠不再能够识别父本和陌生雄鼠的气味；在亲子分开40 d时，雌鼠仍能识别母本和陌生雌鼠的气味。因此，雌鼠对父本气味的嗅觉记忆时间可以持续到亲子分开10—20 d之间；而对母本气味的嗅觉记忆时间则可以持续到亲子分开40 d以上。     

雌性根田鼠断奶后对亲本尿气味的记忆

为研究亲子分开后雌性根田鼠对亲本气味的记忆持续时间,分别在未分开(20日龄)、分开10d(30日龄)、20d(40日龄)、30d(50日龄)、40d(60日龄)时,以新鲜尿作气味源,在行为观察箱中记录雌性根田鼠对不同气味源的行为响应模式,结果表明(1)未分开时,雌鼠遭遇父本气味时自我修饰的频次极显著高于陌生雄鼠气味,在分开10d时,雌鼠接近父本气味的频次显著多于接近陌生雄鼠气味的频次,其对前者反标记显著少于后者;(2)分开20d后,雌鼠对父本和陌生雄鼠气味的行为响应无明显差异;(3)未分窝时,雌性根田鼠幼仔对母本和陌生雌鼠气味的行为响应无差异;(4)分开10—40d时,雌性根田鼠对母本和陌生雌鼠气味表现出不同的行为响应模式。以上结果表明,在亲子分开10d时,雌鼠仍能识别父本和陌生雄鼠的气味;分开20d后,雌鼠不再能够识别父本和陌生雄鼠的气味;在亲子分开40d时,雌鼠仍能识别母本和陌生雌鼠的气味。因此,雌鼠对父本气味的嗅觉记忆时间可以持续到亲子分开10—20d之间;而对母本气味的嗅觉记忆时间则可以持续到亲子分开40d以上。     

根田鼠气味识别的性二型

以新鲜尿和粪作气味源,在行为选择箱中观察根田鼠的行为识别模式,结果表明：雌鼠对陌生同性尿、粪气味源行为识别的差异不显,雄鼠对陌生同性尿、粪气味源的行为识别在多个指标上存在显差异;根田鼠对陌生异性尿、粪的行为响应模式无明显差异;除嗅舔时间外,雌、雄鼠对粪气味的行为识别在其他指标上不存在明显差异;比较雌、雄鼠对尿刺激的行为识别发现,雄鼠对尿刺激的访问频次和反标记显大于雌鼠,雌性嗅舔时间显大于雄性,其他方面二之间并无显差异。因此,雌、雄性根田鼠对粪气味的行为识别模式不存在性别差异;对尿气味的行为识别模式存在性别差异。     

雄性布氏田鼠对不同熟悉程度和动情状态下雌鼠气味的辨别

通过雄性布氏田鼠（Microtus brandti)对配偶和陌生雌鼠气味的辨别实验发现：（1）雌鼠动情状况对雄鼠气味行为反应的影响,当配偶雌鼠处于动情期时,被试雄鼠对动情陌生雌鼠巢垫物的溴闻和舔舐的持续时间都明显多于对非动情陌生雌鼠巢垫物的嗅闻和舔舐时间,而其他行为没有明显判别当配偶雌鼠处于非动情期时,雄鼠对动情的和非动情的陌生雌鼠的气味行为反应都没有明显判别当陌生雌鼠处于动情期时,被试雄鼠对动情配偶气味的嗅闻时间明显多于对非动情配偶的嗅闻时间,而其他行为反应没有明显差异;当陌生雌鼠处于非动情期时,被试雄鼠对动情配偶雌鼠巢垫物的嗅闻时间,挖掘频次,舔舐频次和时间都明显多于对非动情配偶气味的嗅闻,而且雄鼠在动情配偶气味周围搔扒体侧行为的发生频次和持续时间也多于在非动情配偶气味周围的搔扒行为;（2）熟悉性对雄鼠气味行为反应的影响,当配偶雌鼠和陌生雌鼠都处于动情期或都处于非动情期时,被试雄鼠对陌生雌鼠气味的探究行为（嗅问、挖掘和舔噬）和搔扒体侧行为明显多于对配偶雌鼠气味的探究;雄鼠访问陌生雌鼠气味源箱的频次和在其中的停留时间也都多于访问配偶雌鼠气味源箱的频次和停留时间;当配偶雌鼠处于动情期而陌生雌鼠处于非动情期时,被试雄鼠对配偶气味的嗅闻,挖掘和自身修饰行为明显多于对陌生雌鼠气味的行为反应,进入配偶气味源箱中的访问频次也多于进入陌生雌鼠气味源箱的访问频次。结果说明：雌鼠与被试雄鼠的熟悉程度和雌鼠的动情状况直接影响雄性布氏田鼠的社会探究和气味选择行为,即雄鼠偏好并选择动情雌鼠和陌生雌鼠,雄性布氏田鼠对雌鼠气味的行为反应也表现出田鼠属动物典型的多配制种类特征。     

成年布氏田鼠对个体气味信号的识别与记忆

将配对饲养的成年雌雄布氏田鼠分离, 通过分开单独饲养12 h , 1 d、2 d、3 d、5 d 和7 d 后雌、雄鼠对原配偶异性和陌生异性气味信号的选择实验, 探讨布氏田鼠对气味信号的识别和记忆。实验表明: 在分离12 h 和1 d 后, 雄鼠对陌生雌性气味的选择和探究行为显著多于对熟悉雌鼠气味, 而雌鼠对两种气味并未表现显著的探究差异; 布氏田鼠对气味信号的记忆维持的强度和时间随个体不同而产生差异, 雄鼠在分离后12 h、1d、2 d 中对陌生雌鼠气味均表现出差异明显的探究行为, 而后, 各项探究行为的差异均不明显。雌鼠探究行为变化比较缓慢。据此推测雄鼠对气味的记忆维持在2 d 左右。     

雌性布氏田鼠对雄鼠气味的辨别

通过雌性布氏田导其配偶和陌生雄鼠气味的辨别实验,以及无交配经历的成年雌鼠对社会等级不同的陌生雄鼠气的辨别实验发现,有生育经历的雌鼠对陌生雄鼠气味的探究行为明显多于对配偶气味的控究,但雌鼠在配偶雄鼠气味周围的停留时间、自身修饰行为和何处行为的发生频次和持续地陌生雄鼠,没有交配经历的雌鼠对处于从鼠地位的雄性个体气味探究行为多于对优势雄性的控究,而其他行为表现没有明显差异。表明,雌性布氏田鼠可以利用气味     

根田鼠对不同亲属关系异性尿气味的识别

根为检验根田鼠对不同亲属关系异性成体尿气味的识别能力,通过一雄两雌配对实验建立实验种群,从而产生同胞、父系半同胞和陌生个体。在行为选择箱中记录了雌、雄根田鼠对亲属系数分别为0、0.25 和0.5 异性尿气味的行为响应模式。结果如下:雌性根田鼠对3 种不同亲属关系雄鼠气味的接近潜伏期的差异达到极显著水平(P < 0.01),嗅闻时间的差异也达到显著水平(P <0.05),而嗅闻频次和反标记的差异均未达到显著水平(P >0.05)。雄性根田鼠对3 种不同亲属关系雌鼠气味的接近潜伏期和嗅闻时间的差异都未达到显著水平(P >0.05)。对不同亲属关系的气味嗅闻频次和反标记的比较分析表明,三者间的差异也未达到显著水平(P >0.05)。因此,雌性根田鼠能够识别不同亲属关系异性气味并对不同气味表现出不同的行为响应模式;而雄鼠不能识别3 种气味并对其表现出类似的行为模式。     

雌性布氏田鼠对不同共居时间雄性气味的识别与记忆

啮齿动物的社会识别包括对化学信号的辨别、学习和记忆。田鼠属动物雌雄成年个体共居一定时间后,可以利用气味信号来识别配偶。本研究将成年雌雄布氏田鼠配对饲养12 h、18 h、24 h,确认发生交配行为形成配对关系后,分开单独饲养6 h,取配偶雄鼠和陌生雄鼠巢垫物作为个体气味,在气味选择箱中观察雌鼠对配偶雄鼠和陌生雄鼠气味信号的探究和选择行为,从而探讨不同共居时间雌性布氏田鼠对配偶气味信号的识别与记忆的影响。研究结果表明:共居时间影响雌性布氏田鼠对配偶气味的识别与记忆;共居时间越长,雌鼠在气味探究和选择时间上对配偶气味偏好越明显;共居24 h 后,雌性布氏田鼠能够识别出配偶雄鼠的气味信号并形成记忆,这样的记忆维持时间至少是6 h。     

基于交叉抚育的雄性根田鼠对异性同胞尿气味的识别

通过交叉抚育建立室内繁殖种群,在断奶后（80日龄）分别取这些供体的新鲜尿气味作刺激物,在行为观察箱中观察和记录雄性根田鼠对雌鼠气味的行为反应,以研究根田鼠同胞识别的化学通讯机制。结果表明：①在不同的发育时期（2～70日龄）,雄性同巢同胞与异巢同胞的体重没有显著差异。②雄性根田鼠对雌性同巢非同胞气味的接近潜伏期显著长于对异巢非同胞的接近潜伏期（P〈0．05）,其对异巢非同胞气味的访问时间和嗅舔时间都显著高于同巢非同胞气味（P〈0．05）。③雄性根田鼠对雌性异巢同胞和异巢非同胞气味的不存在明显偏好。其对两者的接近潜伏期、访问频次、访问时间、嗅舔频次和嗅舔时间等行为响应均无显著差异（P〈0．05）。这些结果表明,80日龄时,雄性根田鼠能够识别熟悉和陌生的无亲属关系雌性尿气味,但不能区分陌生的亲属和非亲属,因此,其异性同胞识别的机制为共生熟悉模式。     

光周期对雄性布氏田鼠种内个体气味辨别的影响

本文研究了成年雄性布氏田鼠对不同光照周期下(长光照: LD; 短光照: SD) 的陌生雌鼠和陌生雄鼠气味的行为表现。实验发现: 所有被试雄鼠对LD 雄鼠、雌鼠气味比SD 雄鼠、雌鼠气味有更多的社会探究行为。LD 雄鼠比SD 雄鼠对同性或异性陌生个体气味的嗅闻和挖掘行为要多, 而且差异显著。在探究LD 动情雌鼠气味源时, LD 雄鼠比SD 雄鼠表现出更多的嗅闻和挖掘行为; 在探究SD 动情雌鼠气味源时, LD 和SD 雄鼠的行为反应没有明显差别。所有被试雄鼠在LD 雄鼠气味源箱中的停留时间都显著多于在SD 雄鼠气味源箱中的停留时间。LD 雄鼠在LD 雌鼠气味源箱中的停留时间显著多于在SD 雌鼠气味源箱中的停留时间; 而SD 雄鼠在LD 和SD 雌鼠气味源箱中的进入频次和停留时间没有明显差别。同时, LD 雄鼠对LD 动情雌鼠的气味在嗅闻频次和嗅闻时间上多于非动情LD 雌鼠, 而对SD 动情和非动情雌鼠的气味没有表现出明显的偏好; SD 雄鼠对LD 和SD 动情雌鼠的嗅闻行为仅在频次上显著多于对非动情雌鼠的嗅闻, 而在时间上没有显著差别。结果表明: 布氏田鼠嗅觉通讯中的个体气味及其对气味进行辨别过程中的行为反应都随着光照周期的不同而发生变化。动物的个体气味带有季节性信息, 来源于长光照下的气味比短光照下的气味更具有性吸引; 短光照在一定程度上可能抑制了雌鼠的动情和雄鼠的性行为反应。其嗅觉通讯行为的适应意义可能在于: 减少秋季短日照环境下的繁殖活动, 提高雄性个体之间的社会容忍性以利于集群越冬。     

Effects of male rat urine on reproductive and developmental parameters in the dam and her female offspring

This study investigated the direct and indirect effects of male Norway rat (Rattus norvegicus) urine on reproductive, developmental, and fecundity parameters in the dam and her female offspring. Twenty-two dams and litters were studied: 11 in male urine and 11 in distilled water conditions. Only dams were exposed to male urine (or distilled water) from days 14 to 29 postpartum. Significant effects found for the dams exposed to male urine (compared to those only exposed to distilled water) included (i) the second lactational estrus was delayed by 2 days, (ii) vaginal opening and first estrus were 1 day later for female offspring, (iii) the first estrous cycle after vaginal opening was also shorter for their offspring, and (iv) female offspring subsequently produced larger litters than female offspring from dams only exposed to distilled water. Thus, urine from males had direct effects on the timing of the second lactational estrus in dams and indirect effects (mediated by the dam) on developmental and reproductive parameters of her female offspring. Taken as a whole, these results suggest that pheromones in Norway rats may be complex in their effects, context-dependent, and only fully revealed in ecologically relevant contexts. Further study is required to determine whether these effects occur and have biological functions in natural populations.     

Postfledging parental care in Savannah sparrows: sex, size and survival

We investigated postfledging parental care in a philopatric population of Savannah sparrows,Passerculus sandwichensis , breeding on Kent Island, New Brunswick, Canada in an effort to understand the factors influencing adult birds' decisions about parental investment in offspring. Brood division was not based on offspring sex: male and female parents were equally likely to care for sons or daughters. The total duration of parental care, from hatching to independence, was similar for sons and daughters (median=23 days), regardless of the sex of the care-giving parent. The duration of parental care also corresponded closely to the time required for juveniles to acquire basic foraging skills. Despite high levels of extrapair paternity, male Savannah sparrows invested as much in postfledging care and were as effective as females in caring for fledglings, based on recruitment of fledglings into the breeding population the following year. Male parents were more likely to care for smaller fledglings and for offspring from early broods (presumably to enable females to dedicate their efforts towards second clutches). Caring for fledglings was costly for parents: survivorship decreased as a function of the duration of postfledging parental care and the number of fledglings cared for. Parental survivorship, however, was not affected by the sex of the fledglings cared for. This study suggests that sex-biased provisioning may be unlikely except in species with strongly sexually dimorphic offspring, biased offspring sex ratios and sex-biased natal dispersal. Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour.      

First observations of nest attendance behavior by wild maned wolves,Chrysocyon brachyurus

In many species of canids the male's role in reproduction extends to providing extensive or some parental care to his offspring. Maned wolves are a monogamous canid species whose males have been observed providing parental care to their offspring in captivity, but no field observations exist. We observed a wild pair of maned wolves at their nest site in a period soon after the female had given birth for a total period of 65 days. We made five observation sessions with an average of 3–4 days each separated by approximately 2 weeks. Direct visual observations of maned wolves were made each 30 min during the hours of darkness (17:00–07:00) using night-vision binoculars and confirmed by VHF radiotelemetry. During observations we recorded the location of the male and the female in relation to the nest (i.e., in the nest, nearby or long way from the nest). The results showed that the female spent more than 60.44% of her time in or near the nest. The male spent 28.90% of his time in or near the nest. There was a positive significant correlation between the female and the male in terms of the amount of time spent in or near the nest (P<0.01). The maned wolves showed a strong temporal variation in time spent in or near the nest. In conclusion, our data show that wild male maned wolves—probably—provide parental care through provision of food to their female and presumed offspring rather than “babysitting.” Zoo Biol 28:69–74, 2009. © 2008 Wiley-Liss, Inc.     

Paternal Care by Genetic Fathers and Stepfathers II: Reports by Xhosa High School Students

In this article we present a biosocial model of human male parental care that allows relationship (mating) effort to influence male parental allocations. The model recognizes four classes of relationships between men and the children they parent: genetic offspring of current mates (combined relationship and parental effort), genetic offspring of previous mates (parental effort solely), step offspring of current mates (relationship effort solely), and stepchildren of previous mates (essentially no expected investment). We test the model using data on parental investment collected from 340 Xhosa high school students in Cape Town, South Africa. Six measures of paternal investment are examined: the amount of money men spent on students for school, clothing, and miscellaneous expenditures, respectively, and how often men spent time with children, helped them with their homework, or spoke English with them. The tests provide support for the roles of both parental and relationship effort in influencing parental care: men invest significantly more in their genetic offspring and in the children of their current mates. We also examine several proximate influences on parental care, specifically the age and sex of the child, and the percentage of the child's life the father figure coresided with him or her.     

Adaptive secondary sex ratio adjustments via sex-specific infanticide in a bird

Infanticide is easiest to understand when it involves killing the offspring of others [1], but a parent may also kill its own offspring if the sacrifice of currently dependent young leads to higher survival of brood mates [2] or an improvement in the parent's likely future reproduction [3]. However, sex-specific infanticide by parents of their own offspring, although occurring in some human societies [4], is rare across species. Its rarity may be because killing one sex combines wasted parental effort with consequent biases in population sex ratios that are detrimental for the fitness of the overproduced sex [5-7]. We show that killing male offspring can be advantageous to Eclectus parrot (Eclectus roratus) mothers even though frequency-dependent selection then elevates the reproductive value of sons above that of daughters. In poorer-quality nest hollows, broods with a single female nestling had higher reproductive value than broods in which the female had a younger brother. Our data demonstrate frequent targeted removal of male nestlings within 3 days of hatching in these specific brood types and nesting conditions. The ability of Eclectus parrots to perceive the sex of their offspring relatively early may favor decisions to kill one sex before further investment in parental care.     

No evidence for adjustment of sex allocation in relation to paternal ornamentation and paternity in barn swallows

Sex allocation theory predicts that parents should adjust investment in sons and daughters according to relative fitness of differently sexed offspring. In species with female preference for highly ornamented males, one advantage potentially accruing to parents from investing more in sons of the most ornamented males is that male offspring will inherit characters ensuring sexual attractiveness or high-quality genes, if ornaments honestly reveal male genetic quality. Furthermore, in species where extra-pair fertilizations occur, offspring sired by an extra-pair male are expected to more frequently be male than those of the legitimate male if the latter is of lower quality than the extra-pair male. We investigated adjustment of sex ratio of offspring in relation to ornamentation of the extra-pair and the social mate of females by direct manipulation of tails of male barn swallows Hirundo rustica . Molecular sexing of the offspring was performed using the W chromosome-linked avian chromo-helicase-DNA-binding protein (CHD) gene while paternity assessment was conducted by typing of hypervariable microsatellite loci. Extra-pair offspring sex ratio was not affected by ornamentation of their biological fathers relative to the experimental ornamentation of the parental male. Experimental ornamentation of the parental males did not affect the sex ratio of nestlings in their broods. Female barn swallows might be unable to bias offspring sex ratio at hatching according to the quality of the biological father. Alternatively, fitness benefits in terms of sexual attractiveness of sons might be balanced by the cost of compensating for little parental care provided by highly ornamented parental males, if sons are more costly to rear than daughters, or the advantage of producing more daughters, if males with large ornaments contribute differentially more to the viability of daughters than sons.     

How does a parent respond when its mate emphasizes the wrong role? A test using a monogamous fish

The convict cichlid fish, Archocentrus nigrofasciatus, is biparental: the male spends the majority of his time defending the territory and the female spends much of her time close to the offspring. Under natural conditions, this separation into sex-typical roles is somewhat blurred as males do spend some time with the offspring and females do attack intruders. Here we tested whether an individual selects a parental role based on the location (i.e. parental role) of its mate. For example, do females emphasize offspring care because the male is away from the offspring? Will males be more likely to care for the offspring when the female is away from the offspring? We manipulated the location of one parent by placing it in a transparent plastic box, either near the offspring or at the far end of the tank near a clear plastic compartment that held a conspecific male intruder. We tested both male and female parent under the following four conditions: boxed mate near offspring with no intruder present, boxed mate near offspring with intruder present, boxed mate near intruder compartment with no intruder present, and boxed mate near intruder compartment with intruder present. We found that both parents spent more time with the offspring and less time attacking the intruder when the mate was positioned near the offspring and more time away from the offspring and more time attacking the intruder when the mate was near the intruder. Males were more affected by the location of their mates than were females and we concluded that males were attracted both to their mates' location and their offspring while females were mostly attracted to their offspring. Overall, the location of the mate had little effect on the types of aggressive activities used against the intruder. We did find that males increased their aggression towards boxed females when they were positioned far from the offspring, whereas the aggressive behaviour of females towards boxed males when they were positioned near the offspring was ambiguous. We suggest that males in particular enforce the separation of sex-specific parental roles via this aggression.     

Paternal effort and its relation to mating success in the European ground squirrel

The necessity for parental care is a driving force for determining mating systems and social organization. The European ground squirrel, Spermophilus citellus, is a polygynous, gregarious species in which male parental behaviour would not be expected. We had observed males digging in litter burrows that were later occupied by females and their offspring. Males never stayed overnight within these burrows. To determine whether this was some kind of paternal effort we tested the following hypotheses: (1) that male burrowing behaviour was directed towards the male's own offspring or towards the pregnant or lactating mother of the male's offspring; (2) that this behaviour had costs in terms of condition, decreased survival or fecundity; and (3) that it benefited offspring condition or survival. All three assumptions were met. Males worked on the litter burrow of their copulatory partners. Thus, this behaviour was directed towards the male's potential offspring. Male burrowing costs were seen in decreased foraging time and increased body mass loss. Offspring benefits were evident in increased mass at natal emergence. We conclude that male digging at litter burrows can be considered as paternal effort. Lastly, we considered the effects of polygyny on this male parental effort by comparing mating effort, mating success and paternal effort. High mating success was associated with high mating effort and low paternal effort. Moderate to low mating success was associated with lower mating effort and higher paternal effort, indicating a trade-off between the two.     

Paternal Care by Genetic Fathers and Stepfathers I: Reports from Albuquerque Men

We present a biosocial model of human male parental care that allows male parental allocations to be influenced not only by changes in the fitness (welfare) of the recipient offspring, but also by their effects on the man's relationship with the child's mother. The model recognizes four classes of relationships between males and the children they parent: genetic offspring of current mates (combined relationship and parental effort), genetic offspring of previous mates (parental effort solely), step offspring of current mates (relationship effort solely), and stepchildren of previous mates (essentially no expected investment). We test the model using data on parental investments collected from adult males living in Albuquerque, New Mexico, U.S.A. Four measures of paternal investment are examined: the probability that a child attends college (2,191 offspring), the probability that a child who attends college receives money for it (N = 1,212), current financial expenditures on children (N = 635), and the amount of time per week that men spend with children ages 5 to 12 years (N = 2,589). The tests are consistent with a role for relationship effort in parental care: men invest more in the children of their current mates, even when coresidence with offspring is not a confounder.     

A model for evolution of male parental care and female multiple mating

In most animals, males gain a fitness benefit by mating with many females, whereas the number of progeny per female is unlikely to increase as a function of additional mates. Furthermore, males of internally fertilizing species run the risk of investing in offspring of other males if they provide parental care. Nevertheless, males of many avian species and a minority of mammalian species provide parental care, and females of various species mate with multiple males. I investigate a two-locus genetic model for evolution of male parental care and female multiple mating in which females gain a direct benefit by multiple mating from the paternal care they thereby elicit for their offspring. The model suggests that, first, male parental care can evolve when it strongly enhances offspring survival and the direct costs of female multiple mating (e.g., loss of energy, risk of injury, exposure to infectious diseases) are greater than its indirect benefit (e.g., acquisition of good genes, increased genetic diversity among offspring); second, female multiple mating can evolve when paternal care is important for offspring survival or the indirect benefit of multiple mating is larger than its direct cost; and, finally, male parental care and female multiple mating can co-occur.